A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367366



Internal ID21024919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94016371..94022157hg38UCSC Ensembl
chr3:93735215..93741001hg19UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg385787
hg195787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106677
Samples
Known GenesARL13B, STX19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367366
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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